Microstructural Study of Hydration of C3S in the Presence of Calcium Nitrate Using Scanning Transmission X-Ray Microscopy (STXM)

Author:

Li Qinfei123ORCID,Wang Yang1,Geng Guoqing4,Chen Heng13,Hou Pengkun13,Cheng Xin13ORCID,Monteiro Paulo J. M.5,Huang Shifeng13ORCID,Kim Jae Hong6

Affiliation:

1. Shandong Provincial Key Laboratory of Preparation and Measurement of Building Materials, University of Jinan, Jinan, China

2. State Key Laboratory of Green Building Materials, Beijing, China

3. Department of Materials Science and Engineering, University of Jinan, Jinan, China

4. Paul Scherrer Institute, Villigen, Switzerland

5. Department of Civil and Environment Engineering, University of California, Berkeley, USA

6. Department of Civil and Environmental Engineering, Korea Advanced Institute of Science and Technology, Republic of Korea

Abstract

Calcium nitrate (CN) is used widely as an effectively inorganic setting accelerator and antifreeze admixture in concrete structures. In this paper, the multiscale investigation of CN on the hydration of C3S was studied by scanning transmission X-ray microscopy (STXM) combined with near-edge X-ray absorption fine structure (NEXAFS), 29Si MAS NMR, calorimetry, scanning electron microscope, and N2 absorption. It was concluded that the calcium silicate hydrate (C-S-H) surrounds the unhydrated C3S at 1-day hydrated C3S in the presence of calcium nitrate, while portlandite is partly in transformation and is formed partly. Based on Ca L3,2-edge NEXAFS spectra for 1-day hydrated C3S particle, calcium nitrate does not change the structure of the asymmetrically 7-fold coordination of calcium in the C-S-H. Calcium nitrate can accelerate the hydration of C3S to some extent and polymerization of the silicate chains within C-S-H considerably at early age, resulting in the increasing specific surface area.

Funder

U.S. Department of Energy

Publisher

Hindawi Limited

Subject

General Materials Science

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